Informaţii despre

Nume Dysfibrinogenemia
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificare anatomică Malacards Boli de sânge
Boli din aceeaşi familie Dysfibrinogenemia, Congenital

Vezi şi

Boli A-Z Abdominal Tuberculosis Achalasia-Addisonianism-Alacrima Syndrome Acute Liver Failure Adie Pupil Afibrinogenemia Afibrinogenemia, Congenital Aland Island Eye Disease Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha-2-Plasmin Inhibitor Deficiency Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alport Syndrome, X-Linked Amyloidosis Angel-Shaped Phalangoepiphyseal Dysplasia Angina Pectoris Aniridia 1 Anorexia Nervosa 1 Anterior Spinal Artery Syndrome Antiphospholipid Syndrome Antipyrine Metabolism Antithrombin Iii Deficiency Argentine Hemorrhagic Fever Arthritis Arthrochalasia Ehlers-Danlos Syndrome Ascending Cholangitis Ataxia Neuropathy Spectrum Autoimmune Disease Bleeding Disorder, Platelet-Type, 11 Blood Coagulation Disease Blood Group--Ahonen Blood Group, I System Blood Protein Disease Blue Toe Syndrome Budd-Chiari Syndrome Burns Carotid Artery Occlusion Central Retinal Vein Occlusion Cerebral Sinovenous Thrombosis Choledocholithiasis Chronic Thromboembolic Pulmonary Hypertension Compartment Syndrome Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Coronary Thrombosis Cryptogenic Cirrhosis Disseminated Intravascular Coagulation Dysfibrinogenemia, Congenital Eclampsia Eisenmenger Syndrome Encephalopathy, Familial, with Neuroserpin Inclusion Bodies Endocarditis Esophageal Varix Factor V Deficiency Factor Vii Deficiency Factor Viii Deficiency Factor X Deficiency Factor Xi Deficiency Factor Xii Deficiency Factor Xiii Deficiency Fibrinolytic Defect Fournier Gangrene Giant Hemangioma Hellp Syndrome Hematopoietic Stem Cell Transplantation Hemoglobin E Disease Hemophilia B Hemorrhagic Disease Hemorrhagic Fever Hepatic Adenomas, Familial Hepatic Coma Hepatic Tuberculosis Hepatic Vascular Disease Hepatic Veno-Occlusive Disease Hepatitis Hepatitis a Hepatitis E Hepatorenal Syndrome Homocysteinemia Homocystinuria Hypersplenism Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Immune System Disease Inherited Blood Coagulation Disease Intermittent Claudication Intestinal Impaction Intracranial Embolism Intracranial Hypertension Intracranial Thrombosis Ischemia Ischemic Colitis Ischemic Optic Neuropathy Kwashiorkor Lateral Medullary Syndrome Leech Infestation Legg-Calve-Perthes Disease Leukemia Livedoid Vasculopathy Liver Cirrhosis Liver Disease Marantic Endocarditis Meningococcemia Mercury Poisoning Myeloma, Multiple Non-a-E Hepatitis Nonarteritic Anterior Ischemic Optic Neuropathy Ovarian Hyperstimulation Syndrome Pancreatitis Paracetamol Poisoning Paraneoplastic Syndromes Patent Foramen Ovale Peripheral Vertigo Placental Abruption Platelet Aggregation, Spontaneous Porencephaly Portal Vein Thrombosis Postaxial Acrofacial Dysostosis Posterior Myocardial Infarction Post-Thrombotic Syndrome Priapism Protein C Deficiency Protein S Deficiency Prothrombin Deficiency Prothrombin Deficiency, Congenital Pulmonary Embolism Pulmonary Hypertension Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis Purpura Purpura Fulminans Retinal Artery Occlusion Retinal Vascular Occlusion Retinal Vein Occlusion Sagittal Sinus Thrombosis Salt and Pepper Developmental Regression Syndrome Scott Syndrome Severe Pre-Eclampsia Sneddon Syndrome Spinal Cord Infarction Splenic Disease Sticky Platelet Syndrome Stroke, Ischemic Subendocardial Myocardial Infarction Sudden Sensorineural Hearing Loss Thrombophilia Thrombophilia Due to Activated Protein C Resistance Thrombophilia Due to Thrombin Defect Thrombophlebitis Thrombosis Valproate Embryopathy Varicose Veins Vascular Disease Vein Disease Von Willebrand's Disease